Analytical Scientist I: Impurity ID & Method Development

Resolian; Fordham; On-site; GBP 32,000 - 42,000; Full time

Benefits offered by this job

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Job summary

Resolian is seeking a detail-oriented Analytical Scientist to join the Analytical Sciences team in the UK. You will work on cGMP analysis of pharmaceutical samples, develop and validate methods, and identify impurities using LC-MS, GC-MS and ICP-MS while delivering timely, compliant data.

You will follow SOPs, generate reports, and contribute to CAPA and QA audits. Strong communication and organizational skills are essential for success in this role.

Qualifications

• Degree or higher in analytical chemistry, chemistry or related subject.
• Experience in a regulated environment is beneficial.
• Excellent written and verbal communication skills.
• Ability to successfully manage large amounts of information.
• Good organisational skills to perform tasks in a meticulous manner with close attention to detail.
• Flexible attitude to changing priorities and timelines, responding to these challenges positively.
• Good time management skills and ability to work and deliver to tight deadlines.
• Highly motivated and willing to get involved with new initiatives.

Responsibilities

• Work to laboratory SOPs and adhere to cGMP record keeping and procedures.
• Provide right first-time analytical data to agreed schedules using techniques such as LC-MS, GC-MS or other separation techniques.
• Provide verbal and written reports, both internally and externally.
• Get involved in data review and process improvements.
• Contribute to the Quality Assurance programme of laboratory audits, investigations, and CAPA.

Skills

Excellent written/verbal communication

Data handling

Organisational skills

Attention to detail

Time management

Flexible attitude

Motivation to learn

Education

Degree in analytical chemistry or chemistry

Tools

LC-MS

GC-MS

ICP-MS

Job description

Resolian is seeking a detail-oriented Analytical Scientist to join the Analytical Sciences team in the UK. You will work on cGMP analysis of pharmaceutical samples, develop and validate methods, and identify impurities using LC-MS, GC-MS and ICP-MS while delivering timely, compliant data.

You will follow SOPs, generate reports, and contribute to CAPA and QA audits. Strong communication and organizational skills are essential for success in this role.